quality specialist

Parsons

<div>In a world of possibilities, pursue one with endless opportunities. Imagine Next! 

At Parsons, you can imagine a career where you thrive, work with exceptional people, and be yourself. Guided by our leadership vision of valuing people, embracing agility, and fostering growth, we cultivate an innovative culture that empowers you to achieve your full potential. Unleash your talent and redefine what&rsquo;s possible. 
Job Description:
Parsons are seeking an experienced Senior Quality Specialist to ensure the highest standards of quality and compliance in a large-scale airfield/airport development project.
This role requires deep expertise in inspection, testing, and quality assurance of civil infrastructure including runways, taxiways, aprons, pavements, terminals, and supporting structures.
The ideal candidate will have 10+ years of experience in quality assurance within aviation or large infrastructure projects. The Senior Quality Specialist will oversee quality activities, enforce standards, and support timely, safe, and cost-effective project delivery.
What You&rsquo;ll Be Doing:<ul><li>
Develop, implement, and enforce quality control procedures, inspection plans, and testing protocols.</li><li>
Monitor and verify compliance with project specifications, codes, standards, and client requirements.</li><li>
Conduct site inspections and testing of works including runways, taxiways, pavements, foundations, drainage systems, and terminal structures.</li><li>
Prepare detailed inspection reports, non-conformance reports (NCRs), and corrective action plans.</li><li>
Maintain comprehensive quality records and ensure traceability for all works.</li><li>
Provide weekly, monthly, and executive-level quality status updates to project management and stakeholders.</li><li>
Ensure all works comply with local, national, and international standards relevant to airport infrastructure (e.g., ICAO, ASTM, ACI, ISO).</li><li>
Coordinate with design and engineering teams to ensure adherence to specifications.</li><li>
Oversee contractors and subcontractors to ensure works meet quality requirements.</li><li>
Witness, review, and approve testing activities including soil compaction, concrete strength, asphalt quality, and structural inspections.</li><li>
Support troubleshooting and resolution of quality-related issues during construction and commissioning.</li><li>
Ensure that all test results and certifications meet operational and safety requirements.</li><li>
Identify recurring quality issues and recommend corrective and preventive actions (CAPA).</li><li>
Lead quality improvement initiatives and contribute to lessons learned for future airport projects.</li><li>
Promote a culture of safety, quality, and compliance across the civil engineering team.</li><li>
Work closely with engineers, construction teams, procurement, and safety specialists to ensure alignment of quality objectives.</li><li>
Support audits by client representatives, regulatory authorities, and third-party inspection agencies.</li><li>
Coordinate with contractors and suppliers to address quality concerns and implement corrective measures.</li></ul>
What Required Skills You&rsquo;ll Bring:<ul><li>
Bachelor&rsquo;s degree in Engineering or related field.</li><li>
Master&rsquo;s degree preferred.</li><li>
Minimum 10 years of experience in quality assurance/inspection for large infrastructure or airport projects.</li><li>
Strong hands-on experience in runway, taxiway, terminal, pavement, and structural works.</li><li>
Expertise in codes, standards, testing procedures, and quality management systems.</li><li>
Experience with testing and inspection techniques for materials, concrete, asphalt, and earthworks.</li><li>
Excellent documentation, analytical, and reporting skills.</li><li>
Effective communication and leadership skills for coordination with contractors, engineers, and stakeholders.</li><li>
Knowledge of safety regulations and QA/QC procedures for civil construction.</li></ul>
What Desired Skills You&rsquo;ll Bring:<ul><li>
Professional certifications in quality or engineering (e.g., CQA, PE, PMP, ISO Auditor).</li><li>
Familiarity with airport-specific infrastructure including runways, aprons, taxiways, and terminal buildings.</li><li>
Experience with digital quality management tools and reporting platforms.</li><li>
Ability to lead multi-disciplinary teams and manage complex quality challenges in fast-paced environments.</li></ul>
Summary: 
The Senior Quality Specialist will ensure all works in the airport/airfield project adhere to the highest standards of quality, safety, and regulatory compliance. This position requires deep technical expertise, leadership skills, and the ability to implement quality standards across complex infrastructure systems, contributing to successful and timely project delivery.
Parsons equally employs representation at all job levels no matter the race, color, religion, sex (including pregnancy), national origin, age, disability or genetic information.
We truly invest and care about our employee&rsquo;s wellbeing and provide endless growth opportunities as the sky is the limit, so aim for the stars! Imagine next and join the Parsons quest&mdash;APPLY TODAY!<div>
Parsons is aware of fraudulent recruitment practices. To learn more about recruitment fraud and how to report it, please refer to https://www.parsons.com/fraudulent-recruitment/.</div></div>
 <div><div><div>COMPETITIVE BENEFIT OFFERINGS</div></div><div><div><div> 
Financial Wellness</div><div> 
We care about your financial wellbeing. Parsons offers competitive pay and retirement plans to help you build wealth for the future while giving you the flexibility to diversify your investments.</div></div><div><div>
Work Life Harmony</div><div> 
Balance in life is important and time away from the office is imperative to allow you to refresh and focus your attention on the things that matter to you. Parsons supports your time away by providing paid time off and paid flexible holidays.</div></div><div><div>
Career Development</div><div> 
We are committed to fostering the personal and professional growth of our employees. Develop and advance yourself though our comprehensive training, educational and mentorship programs.</div></div><div><div> 
Veteran Support</div><div> 
We provide Industry leading benefits to support veterans and active-duty members to provide security for you and your family by offering robust leave and benefits; including paid active-duty military leave and paid time off when transitioning back to civilian life.</div></div><div><div>
Mind &amp; Body</div><div> 
At Parsons we inspire healthier habits, heathier minds, and a healthier you through our wellness program. Participate in our weekly Meditation Mondays and Wellness Wednesdays. Wellness, at Parsons, is more than just your annual checkup.</div></div><div><div>
Health</div><div> 
Health is not a one size fits all. At Parsons, we offer a robust Employee Assistance Program as well as comprehensive medical, dental and vision plans through large, national carriers with the choice of regional PPO, HDHP, or HMO networks.</div></div></div></div>

Senior Quality Specialist

Stellantis

<div><div>Job ID: 2016694 
Career Area: Quality 
Position Type: Salaried</div>
<div>Location: Headquarters &amp; Technology Center &ndash; Auburn Hills 
48326, US 
Date Posted: April 13, 2026 
Brand: FCA Group</div></div>
 <div>The Corporate Process Quality Specialist is responsible for developing, deploying, auditing, and sustaining corporate-level Manufacturing Quality standards across North American operations. This role supports inspection standards, certification processes, QMS/SIS best practices, reactivity processes, Quality Certification line, Production Quality Gates, Stellantis Customer Audit, and other global/regional quality standards. The specialist serves as a subject-matter expert for process quality, providing hands-on support to assembly plants, conducting process assessments, ensuring regulatory and internal compliance, and driving standardization and continuous improvement.
Deliverables:

Job responsibilities include but are not limited to:
<ul>
<li>Develop, implement, and maintain corporate process and inspection standards</li>
<li>Ensure consistent application of QMS, SIS fundamentals, PQG, SCA, and certification processes across NA plants</li>
<li>Conduct process assessments to validate readiness, robustness, and compliance before process or product changes</li>
<li>Support internal QMS/ISO audits and SIS fundamentals audits</li>
<li>Ensure standards meet regulation, ISO requirements, and company expectations</li>
<li>Develop and sustain Professional Inspection standards and best practices.</li>
<li>Support Certification Line processes and government/regulatory practices related to manufacturing quality</li>
<li>Execute or support process quality tasks within BIW, Paint, and General Assembly, including online inspection, torque auditing, control plans, PFMEAs, and traceability</li>
<li>Analyze internal/external quality indicators to identify trends and validate quality control effectiveness</li>
<li>Review and interpret MCV (Palantir) data to verify process performance</li>
<li>Lead robust root-cause analysis activities to resolve issues and prevent recurrence</li>
<li>Recommend and implement mistake-proofing and cost-effective quality improvements</li>
<li>Represent the Voice of the Customer by ensuring customer-focused quality practices</li>
<li>Support launch readiness and implementation of new methodologies in assembly manufacturing facilities</li>
<li>Provide training and coaching on inspection standards, QMS/SIS best practices, and process quality expectations for hourly and salaried employees</li>
<li>Share best practices globally to ensure alignment with North American process integrity</li></ul></div>
 <div>EOE/Disability/Veteran
At Stellantis, we assess candidates based on qualifications, merit, and business needs. We welcome applications from all people without regard to sex, age, ethnicity, nationality, religion, sexual orientation, disability, or any characteristic protected by law. We believe that diverse teams reflect our identity as a global company, enabling us to better address the evolving needs of our customers and care for our future.
Our benefits reflects the STELLANTIS commitment to helping you reach your personal and professional goals. In addition to an environment that promotes career development, we offer benefits for a healthy lifestyle and a rewarding future, designed to take care of you and your family, in various stages of life.

As a global company, our employee packages will vary by country, customary norms and the legal entity into which you are hired.

We care about your privacy. For more information on how your personal data is processed, please read the specific Privacy Statement provided by the respective entities whose job offer you have selected.</div>

Corporate Process Quality Specialist

Arkana Laboratories

<div><div>Who we are: At Arkana Laboratories, everyone has an important role to fill. Come join us and be a part of a team dedicated to making life better for those who need it most.

This place is packed with super-smart people who do their best work together. We work hard every day to advance our understanding of disease and provide world-class care to our patients in hopes of leaving our corner of the world a little better than we found it. While we are committed to improving the lives of thousands of patients, we never lose sight of the realization that they are the reason we get to create change in our field.

Built on generosity, teamwork, and the freedom to try new things, we take great pride in our work. Great ideas come from everywhere in this company and we celebrate each success and failure for the opportunity it gives us to keep reaching. For more than twenty years after our founder, Dr. Patrick Walker, wrote his goals on the back of a napkin, our people, culture, and values have remained strong.</div>
About the position: As the Clinical Data Quality Specialist, you will ensure the integrity and clinical validity of laboratory data while supporting AI/ML initiatives through expert annotation and data curation. This role represents a fundamental transformation from traditional documentation functions to modern data operations, requiring individuals who embrace change, demonstrate initiative, and are committed to continuous learning. This position bridges clinical knowledge and data science, transforming healthcare data into high-quality assets that power analytics, research, and artificial intelligence applications. Success requires adaptability, technical curiosity, and the ability to work independently in an evolving environment.

What you'll do:

Data quality and validation
<ul>
<li>Review and audit laboratory data for accuracy, completeness, and clinical validity
</li>
<li>Identify and resolve data inconsistencies and quality issues
</li>
<li>Validate automated processes and ensure alignment with quality standards
</li>
<li>Support development of data quality metrics and tracking tools
</li>
</ul>Clinical data annotation and curation
<ul>
<li>Annotate and categorize clinical data to support machine learning models
</li>
<li>Apply medical terminology and clinical knowledge to ensure accuracy
</li>
<li>Maintain consistency and meet established accuracy standards
</li>
<li>Contribute to data dictionaries and documentation standards
</li>
</ul>Automation and process improvement
<ul>
<li>Monitor automated workflows and identify opportunities for improvement
</li>
<li>Support testing and validation of new systems and tools
</li>
<li>Recommend enhancements to improve efficiency and data quality
</li>
</ul>Collaboration and communication
<ul>
<li>Partner with data science, IT, and laboratory teams on cross-functional projects
</li>
<li>Provide clinical context to support technical initiatives
</li>
<li>Participate in team knowledge sharing and process development
</li>
</ul>Continuous development
<ul>
<li>Complete training in data quality, systems, and clinical informatics
</li>
<li>Stay current with trends in healthcare data and technology
</li>
<li>Take initiative in learning new tools and expanding skill sets
</li>
<li>Perform other duties as assigned
</li>
</ul>What you bring:
<ul>
<li>Strong attention to detail and analytical thinking
</li>
<li>Ability to work independently and take initiative
</li>
<li>Comfort working in a changing and evolving environment
</li>
<li>Strong communication and collaboration skills
</li>
<li>Curiosity and interest in data, technology, and process improvement
</li>
</ul>Qualifications
<ul>
<li>High school diploma or GED required; associate degree or higher preferred
</li>
<li>Two or more years of experience in healthcare documentation, medical records, laboratory operations, or a related field
</li>
<li>Experience with EHR, LIS, or similar systems
</li>
<li>Proficiency in Microsoft Excel and general computer applications
</li>
<li>Knowledge of medical terminology and healthcare workflows
</li>
<li>Understanding of HIPAA and data confidentiality requirements
</li>
</ul>Preferred qualifications
<ul>
<li>Certification such as RHIT, RHIA, or CCA, or willingness to pursue
</li>
<li>Exposure to data analysis tools, SQL, or reporting platforms
</li>
<li>Experience with quality audits or data validation processes
</li>
</ul>Schedule: Monday-Friday 8am-5pm<div>
What we offer: We know that health is more than doctor visits and life is more than work. We work hard at Arkana but in turn provide competitive salaries and generous benefit offerings.

Specifically, we offer the following benefits to full-time employees:
<ul>
<li>Competitive salary</li>
<li>Generous paid time off and Paid Holidays</li>
<li>Minimal cost health insurance for you and affordable options for your family</li>
<li>401(k) with immediate eligibility and match</li>
<li>Company-paid life insurance</li>
<li>Company-paid long term disability coverage</li>
<li>Affordable vision and dental plans</li>
<li>Flexible Spending Account or Health Savings Account availability</li>
<li>Wellness plan and complimentary yoga classes</li>
<li>Monthly in-office massages and employer-sponsored lunches</li>
</ul>
Please see Careers for further information.</div></div>

Clinical Data Quality Specialist

Arizona Arthritis and Rheumatology

<div>Description:

Our providers work together to keep patients healthy and are recognized for excellence in medicine and for being pioneers in new treatments, ably supported by our Research department.
We are an equal employment opportunity employer and will consider all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability.
Our vision is to provide the best Rheumatology care, anywhere and, to balance sustainable operation with the highest possible level of patient care.
We are a seeking an ambitious, friendly, positive, and compassionate Clinical Research Systems Quality Specialist to join our team.
Under minimal supervision, the System Quality Specialist (SQS) owns and improves the quality, integrity, and compliance readiness of clinical research electronic systems (e.g., CTMS, eSource/EDC, eRegulatory, M365, and related reporting tools). The SQS defines data quality standards and controls, manages system change control and quality validation/testing, monitors system performance using dashboards and metrics, and maintains audit-ready documentation (SOPs, training records, configuration and validation evidence). The SQS partners with cross-functional stakeholders to implement study builds and amendments, communicate system updates, ensure appropriate access controls, and drive corrective/preventive actions to prevent recurring system and data quality issues.
RESPONSIBILITIES<ul><li>
Establish and maintain system quality management practices for clinical research platforms (e.g., CTMS, eSource/EDC, eRegulatory, M365), including documentation standards, validation evidence, and release readiness criteria</li><li>
Ensure architecture and data inputs for systems below continuously meet or exceed minimum quality standards</li><li>
Clinical Conductor CTMS</li><li>
Advarra eSource +EDC</li><li>
Veeva SiteVault eReg</li><li>
Monday Work Management</li><li>
SharePoint Pages &amp; Training Workflows</li><li>
Power Query/BI Dashboards</li><li>
in the CTMS system for both protocol and financial compliance</li><li>
Review, finalize and approve esource and CTMs builds for all new studies and amendments</li><li>
Ensure all systems are updated when amendments occur and announce changes to stakeholders</li><li>
Perform routine quality inspections of system data inputs for compliance with internal policy, standard operating procedures, ICH-GCP Standards, local and FDA regulations</li><li>
Ensure all system quality controls are in place prior to release (e.g., procedural instructions, conditional/required fields, data constraints, standardized build templates, and controlled vocabularies) to reduce downstream queries and protocol deviations</li><li>
Perform root cause analysis for recurring system/data quality issues; lead remediation plans to prevent reoccurrence (process, training, configuration, or automation changes)</li><li>
Maintain dashboards/metrics (e.g., query rates, missing/late data, build defect rates, timeliness KPIs) and drive corrective/preventive actions</li></ul>
Learn more about AARA on our website at http://azarthritis.com
Requirements:

QUALIFICATIONS<ul><li>
Bachelor&rsquo;s Degree or equivalent</li><li>
2 years clinical research coordinator experience</li><li>
Rheumatology Experience Preferred</li><li>
Must be able to sit for long periods of time</li><li>
Demonstrated experience applying quality controls to electronic clinical research systems to ensure accurate, complete, and timely data</li><li>
Expensive working knowledge of relevant electronic systems, including eSource, CTMS, eReg, and Microsoft 365</li><li>
Strong understanding of good clinical practice, FDA regulations, &amp; data integrity principles (e.g., ALCOA/C+) with an ability to translate them into system configuration, workflows, and user guidance</li><li>
Proficiency building and interpreting operational quality metrics and dashboards</li></ul></div>

Clinical Research Systems Quality Specialist

HOF Immigration Services

Job OverviewWe are looking for a sharp, detail-oriented Call Quality Assurance Specialist to join our operations team. You will be the ears of the business &mdash; listening to calls, ensuring our team is following the right processes, and helping us continuously raise the bar on client communication.What You Will Do<ul><li>Monitor and evaluate recorded and live calls against HOF Migration's SOPs and internal quality manual</li><li>Score calls using a structured evaluation scorecard and maintain accurate records</li><li>Identify patterns, recurring errors, and compliance gaps across the team</li><li>Escalate calls involving serious breaches, incorrect advice, or unprofessional conduct</li><li>Provide clear, constructive written feedback to team leaders and HR</li><li>Prepare daily and weekly quality reports for management</li><li>Track and analyze performance metrics (conversion quality, CSAT, compliance adherence)</li><li>Ensure adherence to data privacy and client confidentiality standards</li></ul>Who We Are Looking For<ul><li>Bachelor&rsquo;s degree in Business, Communications, HR, or related field</li><li>2&ndash;4 years of experience in call quality assurance, call monitoring, or a customer service environment</li><li>Excellent written and verbal communication in English</li><li>Strong understanding of call center KPIs and QA frameworks</li><li>Excellent listening, auditing, and analytical skills</li><li>Comfortable working with MS Excel or Google Sheets for logging and reporting</li><li>Highly organized, objective, and able to work independently</li><li>Trustworthy and discreet when handling sensitive client information</li></ul>Working Hours: 11:00 AM &ndash; 8:00 PM (Monday-Saturday)Work Location: In person

Call Quality Assurance Specialist

VITROLIFE

<div>At the Vitrolife Group, we work every day to unlock the full potential of science and technology to reduce the barriers towards building a family. Together we help our customers and their patients to fulfill the dream of having a baby. 
Make Quality Matter &mdash; Where It Impacts Lives.
We are looking for a Quality Assurance Specialist to strengthen and advance our local quality operations in Riyadh. This role sits at the intersection of regulatory excellence, operational quality, and continuous improvement, ensuring that our laboratory services meet the highest international and local standards.
You will play a key role in driving compliance, enabling safe and effective services, and embedding a proactive quality culture &mdash; working closely with both local teams and regional quality leadership.<h4 class="jobSectionHeader"> 
Your Impact</h4>
As a Quality Assurance Specialist, you will:<h6 class="jobSectionHeader">
Drive Quality Operations &amp; Compliance</h6><ul><li>
Oversee day-to-day quality activities and ensure adherence to local and regional requirements</li><li>
Maintain accurate quality records and actively participate in quality management forums</li><li>
Ensure compliance with MOH, SFDA, CBAHI, and other applicable regulations</li></ul><h6 class="jobSectionHeader">
Strengthen the Quality Management System (QMS)</h6><ul><li>
Manage document control processes to ensure procedures are current, compliant, and accessible</li><li>
Support implementation and updates of local and global procedures</li><li>
Contribute to continuous improvement of QMS processes</li></ul><h6 class="jobSectionHeader">
Lead Audits, Risk &amp; Continuous Improvement</h6><ul><li>
Plan and conduct internal audits; manage findings and CAPA implementation</li><li>
Support external audits and regulatory inspections</li><li>
Lead local risk assessments and foster a proactive risk management culture</li></ul><h6 class="jobSectionHeader">
Manage Deviations, CAPA &amp; Performance</h6><ul><li>
Investigate deviations and ensure effective CAPA closure</li><li>
Monitor KPIs, incidents, and nonconformities</li><li>
Identify trends and escalate critical insights to Regional Quality Management</li></ul><h6 class="jobSectionHeader">
Enable Regulatory &amp; Operational Excellence</h6><ul><li>
Monitor regulatory changes and ensure timely implementation</li><li>
Support licensing, certifications, and renewals</li><li>
Ensure quality alignment in new or modified services</li></ul><h6 class="jobSectionHeader">
Collaborate &amp; Build Capability</h6><ul><li>
Train and support staff on quality and regulatory requirements</li><li>
Evaluate the external critical suppliers/service provider and referral laboratories to ensure compliance</li><li>
Contribute to regional and global quality initiatives and harmonization efforts</li></ul><h4 class="jobSectionHeader">
Who You Are</h4>
You are a structured, analytical, and proactive quality professional who thrives in regulated environments and enjoys collaborating across teams.<h4 class="jobSectionHeader">
Qualifications</h4><ul><li>
Bachelor&rsquo;s degree in Laboratory Sciences, Biomedical Sciences, or related field</li><li>
SCFHS license (preferred)</li><li>
Certification in Quality Assurance or Regulatory Affairs is a plus</li></ul><h4 class="jobSectionHeader">
Experience</h4><ul><li>
3&ndash;4 years in a similar QA/regulatory role</li><li>
Experience within laboratory or medical environment</li><li>
Strong knowledge of:<ul><li>
MOH and SFDA regulations (required)</li><li>
CBAHI standards (required)</li><li>
ISO 15189 and CAP accreditation (preferred)</li></ul></li></ul><h4 class="jobSectionHeader">
Skills</h4><ul><li>
Strong understanding of QMS, audits, and documentation</li><li>
Experience with QMS/LIS systems</li><li>
Excellent problem-solving and organizational skills</li><li>
Strong communication and collaboration abilities</li><li>
Fluent in Arabic and English (written and spoken)</li></ul><h4 class="jobSectionHeader">
What You Bring Beyond the Basics</h4><ul><li>
A proactive mindset &mdash; you don&rsquo;t wait for issues, you prevent them</li><li>
The ability to translate regulations into practical, working processes</li><li>
Confidence to challenge, improve, and influence</li><li>
A strong sense of ownership and accountability</li></ul><h4 class="jobSectionHeader">
Why Join Us</h4><ul><li>
Be part of an organization where quality is central to patient impact</li><li>
Work in a collaborative regional and global environment</li><li>
Contribute to high-standard laboratory services and continuous improvement</li><li>
Grow within a culture that values expertise, structure, and innovation</li></ul><h6 class="jobSectionHeader">
Additional Information</h6><ul><li>
Preference will be given to Saudi Nationals</li></ul>
Vitrolife Group is a global provider of medical devices and genetic services. Based on science and advanced research capabilities, we develop services and products for personalized genetic information and medical device products. We support our customers by improving their clinical practice for the patient's outcome of fertility treatment.
We are currently approximately 1 100 colleagues worldwide, with headquarters in Gothenburg, Sweden. Vitrolife Group's products and services are available in more than 110 countries through our own presence in 30 countries and a network of distributors. Vitrolife Group is a sustainable market leader and aims to be the preferred partner for IVF-clinics by providing superior products and services with the vision of fulfilling the dream of having a baby. The Vitrolife share is listed on Nasdaq Stockholm.</div>

Quality Assurance Specialist

Qatar Living®

<div>
 
 
 About Qatar Living
 
 
 
 
 
 
 Qatar Living is Qatar's largest and most trusted digital classifieds platform, serving over 1 million monthly users across Properties, Jobs, Vehicles, and Classifieds. Our technology team is growing fast, shipping new features across a Next.js web platform, React Native mobile apps (iOS &amp; Android), and a NestJS microservices backend. Quality is not an afterthought here; it is a core part of how we ship.
 
 
 
 
 
 
 Role Overview
 
 
 
 
 
 
 We are looking for a mid-level QA Specialist who can operate across the full testing spectrum, from hands-on manual exploratory testing to building and maintaining automated test suites. You will be embedded within our product and engineering squads, responsible for ensuring that every release across web, mobile, and API meets the highest quality bar before it reaches our users.
 
 
 
 
 
 
 Key Responsibilities
 
 
 
 
 
 
 
 Manual Testing
 
 
 <ul>
 <li>
 Design, write, and execute detailed test cases and test plans for new features and bug fixes across web, mobile, and API.
 </li>
 <li>
 Perform exploratory, regression, functional, and UAT testing across all platforms before each release.
 </li>
 <li>
 Test responsive web behavior across browsers and devices; validate iOS and Android app builds via TestFlight and Google Play internal testing.
 </li>
 <li>
 Identify, document, and track bugs with clear reproduction steps, severity ratings, and supporting evidence (screenshots, logs, videos).
 </li>
 <li>
 Collaborate closely with developers and product managers to clarify requirements and catch gaps before development begins.
 </li>
 <li>
 Validate fixes and perform sign-off testing to confirm defect resolution.
 </li>
 </ul>
 
 
 
 
 
 Test Automation
 
 
 <ul>
 <li>
 Build, maintain, and expand automated test suites covering critical user flows across web and mobile.
 </li>
 <li>
 Write automation scripts for end-to-end, regression, and smoke test coverage using industry-standard frameworks.
 </li>
 <li>
 Integrate automated tests into the CI/CD pipeline to enable automated testing on every deployment.
 </li>
 <li>
 Monitor test results, triage failures, and ensure the test suite stays healthy and trustworthy.
 </li>
 <li>
 Identify which test cases deliver the highest ROI for automation and prioritize accordingly.
 </li>
 </ul>
 
 
 
 
 
 API Testing
 
 
 <ul>
 <li>
 Test REST APIs across all backend microservices, validating request/response schemas, status codes, error handling, and edge cases.
 </li>
 <li>
 Write and maintain automated API test collections covering happy paths, failure scenarios, and boundary conditions.
 </li>
 <li>
 Verify data integrity between frontend interfaces and backend services.
 </li>
 <li>
 Test authentication flows, rate limiting, and permission-based access controls at the API layer.
 </li>
 </ul>
 
 
 
 
 
 Quality Process &amp; Reporting
 
 
 <ul>
 <li>
 Maintain a structured test repository, organized, versioned, and accessible to the entire team.
 </li>
 <li>
 Produce clear QA reports per sprint: test coverage, pass/fail rates, open defects, and release readiness assessments.
 </li>
 <li>
 Participate in sprint ceremonies, planning, reviews, and retrospectives, as the quality voice in the room.
 </li>
 <li>
 Proactively flag quality risks before they become production incidents.
 </li>
 <li>
 Contribute to improving QA processes, standards, and team practices over time.
 </li>
 </ul>
 
 
 
 
 
 Qualifications &amp; Requirements:
 
 
 
 
 
 <ul>
 <li>
 Bachelor's degree in Computer Science, Software Engineering, or a related field.
 </li>
 <li>
 ISTQB certification is a plus .
 </li>
 <li>
 3&ndash;6 years of hands-on QA experience covering both manual and automated testing.
 </li>
 <li>
 Strong experience writing test cases, test plans, and bug reports, clear, structured, and actionable.
 </li>
 <li>
 Hands-on automation experience with at least one framework (Playwright, Selenium, Cypress, Appium, or equivalent).
 </li>
 <li>
 Solid API testing experience using tools like Postman, REST Assured, or similar.
 </li>
 <li>
 Mobile testing experience on both iOS and Android, including device farm or emulator-based testing.
 </li>
 <li>
 Familiarity with CI/CD pipelines and integrating tests into automated build processes.
 </li>
 <li>
 Experience working in Agile/Scrum teams with sprint-based delivery cycles.
 </li>
 <li>
 Strong attention to detail and an instinct for breaking things before users do.
 </li>
 </ul>
 
 
 
 
 
 Nice-to-Have
 
 
 <ul>
 <li>
 Experience testing classifieds, marketplace, or e-commerce platforms.
 </li>
 <li>
 Familiarity with performance or load testing (k6, JMeter, or similar).
 </li>
 <li>
 Basic understanding of React Native or Next.js to better communicate with developers.
 </li>
 <li>
 Exposure to accessibility testing standards (WCAG).
 </li>
 <li>
 Arabic language skills are a plus.
 </li>
 </ul>
 
 
</div>

Search 10000+ Quality specialist jobs near you this May. New roles added regularly across leading industries. Apply today.

10000 quality specialist jobs Near Me

Senior Quality Specialist

Corporate Process Quality Specialist

Clinical Data Quality Specialist

Clinical Research Systems Quality Specialist

Call Quality Assurance Specialist

Quality Assurance Specialist

Quality Assurance Specialist